CH180691A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH180691A CH180691A CH180691DA CH180691A CH 180691 A CH180691 A CH 180691A CH 180691D A CH180691D A CH 180691DA CH 180691 A CH180691 A CH 180691A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- preparation
- dye
- parts
- dyeing
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Azofarbstoffes. Es wurde gefunden, dass man einen wert vollen Azofarbstoff erhält, wenn man die Diazoverbindung des 5-Nitro-2-amino-l-oxy- benzols mit 1-N-Oxäthyl-N-butylamino-3- methylbenzol kuppelt.
Der Farbstoff eignet sich vorzüglich zum Färben von Zelluloseestern und -äthern aus wässrigem Bade und liefert hierbei blau stichig fuchsinrote Färbungen, die sich durch besondere Klarheit und gute Lichtechtheit auszeichnen, sowie waschecht und rein weiss ätzbar sind; er eignet sich ferner zum Fär ben von Harz- und Nitrozelluloselacken.
<I>Beispiel</I> 154 Teile 5-Nitro-2-amino-l-oxyberrzol werden in 6000 Teilen Wasser suspendiert, mit 250 Teilen 35 /oiger, Salzsäure versetzt und unter allmählicher Zugabe von 300 Tei len einer 23 0%igen Natriumnitritlösung diazo- tiert. Die so erhaltene Lösung der Diazover- bindung wird mit einer Lösung von 218 Teilen 1-N-Oxäthyl-N-butylamino-3-methyl- Benzol in 120 Teilen 35
%iger Salzsäure und 1000 Teilen Wasser bei 40 bis 50 0 C gekup pelt. Die Farbstoffbildung wird durch Zugabe von 500 Teilen Natriumacetat zu Ende geführt.
Process for the preparation of an azo dye. It has been found that a valuable azo dye is obtained if the diazo compound of 5-nitro-2-amino-1-oxybenzene is coupled with 1-N-oxethyl-N-butylamino-3-methylbenzene.
The dye is particularly suitable for dyeing cellulose esters and ethers from aqueous baths and provides blue-tinged fox-red dyeings, which are characterized by particular clarity and good lightfastness, and are washable and can be etched in pure white; it is also suitable for dyeing resin and nitrocellulose lacquers.
<I> Example </I> 154 parts of 5-nitro-2-amino-1-oxyberrzene are suspended in 6000 parts of water, 250 parts of 35% hydrochloric acid are added and 300 parts of a 23% strength are gradually added Diazotized sodium nitrite solution. The solution of the diazo compound thus obtained is mixed with a solution of 218 parts of 1-N-oxethyl-N-butylamino-3-methylbenzene in 120 parts
% hydrochloric acid and 1000 parts of water at 40 to 50 0 C gekup pelt. The dye formation is brought to an end by adding 500 parts of sodium acetate.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE180691X | 1934-03-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH180691A true CH180691A (en) | 1935-11-15 |
Family
ID=5712340
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH180691D CH180691A (en) | 1934-03-09 | 1935-02-06 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH180691A (en) |
-
1935
- 1935-02-06 CH CH180691D patent/CH180691A/en unknown
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